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Items: 12

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    Number of Variants: 12

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3873515copy number variation1nstd102humanBenign GRCh37 chr6: 37,851,595-37,852,459 , GRCh38.p12 chr6: 37,883,819-37,884,683 ZFAND3
    nsv3919034copy number variation1nstd102humanBenign NCBI36 chr6: 38,157,563-38,710,042 , GRCh37 chr6: 38,049,585-38,602,064 , GRCh38 chr6: 38,081,809-38,634,288 BTBD9, TFGP1, 3 more genes
    nsv3871326copy number variation1nstd102humanUncertain significance GRCh37 chr6: 37,684,241-37,951,820 , GRCh38.p12 chr6: 37,716,465-37,984,044 ZFAND3, RNVU1-33, 2 more genes
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv6290922copy number variation1nstd102humanUncertain significance GRCh37 chr6: 37,485,973-38,275,476 , GRCh38.p12 chr6: 37,518,197-38,307,700 RN7SL285P, ZFAND3-DT, 7 more genes
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